VISERA™ Imaging System
In plain language
This recall involves the VISERA Imaging System - Valve and MAJ-1218 Biopsy Valve sold in Canada. It's being recalled because rubber fragments may detach from the device. Olympus is investigating this issue and will provide an updated notification by mid-2026.
What to do
- Contact the manufacturer if you require additional information.
- Adhere strictly to the Instructions for Use (IFU).
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Affected products
VISERA Imaging System - Valve
Lot: All lots.
MAJ-1218 Biopsy Valve
Model: MAJ-1218
Lot: All lots.
MAJ-210
Model: MAJ-210
Lot: All lots.
Why this matters
Rubber fragment detachment
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: MAJ-1218, MAJ-210
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Rubber fragment detachment
What should consumers do?
Contact the manufacturer if you require additional information. Adhere strictly to the Instructions for Use (IFU).
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Rubber fragment detachment
When was this product recalled?
This product was recalled on February 10, 2026.
Is the OLYMPUS MEDICAL SYSTEMS CORP. brand affected by this recall?
Yes, OLYMPUS MEDICAL SYSTEMS CORP. products are affected by this recall. This recall involves the VISERA Imaging System - Valve and MAJ-1218 Biopsy Valve sold in Canada. It's being recalled because rubber fragments may detach from the device. Olympus is investigating this issue and will provide an updated notification by mid-2026.